Genes A, B, C, and D are linked. The distances between the genes are:
Relationship Map Unit
D – A 11
D – B 7
D – C 22
B – C 15
A – B 4
What is the order of the genes on the chromosome?
1. D B A C
2. D B C A
2. D C B A
4. A B C D

Subtopic:  Recombination Gene Mapping |
 93%
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A woman whose father was colorblind marries a normal man. What are the chances that their son would have colorblindness?
1. 0%
2. 25%
3. 50% 
4. 100%
Subtopic:  Mendelian Disorders |
 73%
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A change in chromosome number, where the changed number is not an exact multiple of the base number N, is called as:
1. Polyteny 2. Aneuploidy
3. Polyploidy 4. Euploidy
Subtopic:  Non - Disjunction & Aneuploidy | Chromosomal Disorders |
 82%
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Consider the given two statements.
Statement I: It is not necessary that the dominant allele will be the most common allele in a population.
Statement II: Dominance is not an autonomous feature of an allele.
1. Only Statement I is correct.
2. Only Statement II is correct.
3. Both Statement I and Statement II are correct.
4. Both Statement I and Statement II are incorrect.
Subtopic:  Monohybrid Cross: 1 |
 80%
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Which of the following best explains a frequency of recombination of 50% in a dihybrid test cross?
1. The two genes are likely to be located on different chromosomes.
2. All of the offspring have combinations of traits that match one of the two parents.
3. The genes are located on sex chromosomes.
4. Abnormal meiosis has occurred.
Subtopic:  Linkage | Recombination Gene Mapping | Recombination & Gene Mapping |
 59%
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Which of the following statements correctly describes the difference between incomplete dominance and co-dominance?
1. Incomplete dominance results in progeny not resembling either of the parents, whereas co-dominance results in progeny resembling both parents.
2. Incomplete dominance involves multiple alleles, while co-dominance does not.
3. Co-dominance occurs in phenotypes only, while incomplete dominance occurs in genotypes.
4. Incomplete dominance is a type of sex-linked inheritance, whereas co-dominance occurs in autosomes.
Subtopic:  Dominance Deviation from Mendel: 1 |
 98%
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Assertion (A):  Pure lines breed true.
Reason (R): Pure lines are heterozygous for the trait.
 
1.  Both (A) and (R) are True and (R) correctly explains (A)
2. Both (A) and (R) are True but (R) does not correctly explain (A)
3. (A) is True, (R) is False
4. (A) is False, (R) is False
Subtopic:  Introduction to Genetics: 1 |
 88%
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Consider the given two statements:
Assertion (A): Scientifically, it is correct to say that the sex of the baby is determined by the father and not by the mother in humans.
Reason (R): In humans, the males are homogametic but the females are heterogametic.
  
1. Both (A) and (R) are True and (R) correctly explains (A)
2. Both (A) and (R) are True but (R) does not correctly explain (A)
3. (A) is True (R) is False
4. (A) is False (R) is True
Subtopic:  Sex Determination |
 93%
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Consider the given two statements:
Statement I: Bateson and Punnett gave the chromosomal theory of inheritance.
Statement II: de Vries, Correns and Tschermak rediscovered Mendel’s laws.
 
1. Statement I is correct; Statement II is correct
2. Statement I is incorrect; Statement II is correct
3. Statement I is correct; Statement II is incorrect
4. Statement I is incorrect; Statement II is incorrect
Subtopic:  Chromosomal Basis of Inheritance: Introduction |
 91%
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What is the probability of having a child with a medium skin color in humans if both parents are heterozygous (AaBbCc)?
1. 1/64 2. 6/64
3. 15/64 4. 20/64
Subtopic:  Polygenic Inheritance & Pleiotropy |
From NCERT
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